Literature DB >> 8777555

Living with epilepsy: a qualitative study investigating the experiences of young people attending outpatients clinics in Leicester.

M Wilde1, C Haslam.   

Abstract

Epilepsy is a disorder associated with significant psychosocial morbidity, and the effects of a stigmatizing condition upon the everyday life and adjustment of young people is not known. The study involved in-depth interviews with 24 young people (15 females, 9 males), aged between 13 and 25 years, all of whom suffered from epilepsy and attended outpatients clinics. The important issues raised included the finding that a large proportion of the sample (71%) reported having been the victims of prejudice, especially bullying and teasing while they were at secondary school. Additionally, many subjects were critical of the medical profession and support services for people with epilepsy, complaining that they were not meeting their needs appropriately. Most subjects reported feelings of apprehension about telling others about their epilepsy, especially members of the opposite sex, and potential employers. Most described supportive, positive relationships with their families and close friends, and parental overprotection was rarely reported by them as being a significant problem. In addition, an estimate of subjects' adjustment to epilepsy was obtained which appears to indicate that the majority were coping well with their condition, even though it may have been resented by some of them.

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Mesh:

Year:  1996        PMID: 8777555     DOI: 10.1016/s1059-1311(96)80065-3

Source DB:  PubMed          Journal:  Seizure        ISSN: 1059-1311            Impact factor:   3.184


  6 in total

Review 1.  NICE guidelines and the epilepsies: how should practice change?

Authors:  C Dunkley; J H Cross
Journal:  Arch Dis Child       Date:  2006-06       Impact factor: 3.791

2.  Behavior and mental health problems in children with epilepsy and low IQ.

Authors:  Janice M Buelow; Joan K Austin; Susan M Perkins; Jianzhao Shen; David W Dunn; Philip S Fastenau
Journal:  Dev Med Child Neurol       Date:  2003-10       Impact factor: 5.449

Review 3.  Knowledge and information needs of young people with epilepsy and their parents: Mixed-method systematic review.

Authors:  Sheila A Lewis; Jane Noyes; Stephen Mackereth
Journal:  BMC Pediatr       Date:  2010-12-31       Impact factor: 2.125

4.  Effective process or dangerous precipice: qualitative comparative embedded case study with young people with epilepsy and their parents during transition from children's to adult services.

Authors:  Sheila A Lewis; Jane Noyes
Journal:  BMC Pediatr       Date:  2013-10-16       Impact factor: 2.125

5.  Social Behavioral Problems and the Health-Related Quality of Life in Children and Adolescents with Epilepsy.

Authors:  Hee-Yeon Choi; Song E Kim; Hyang Woon Lee; Eui-Jung Kim
Journal:  Psychiatry Investig       Date:  2016-09-30       Impact factor: 2.505

Review 6.  Classifying epilepsy pragmatically: Past, present, and future.

Authors:  Nathan A Shlobin; Gagandeep Singh; Charles R Newton; Josemir W Sander
Journal:  J Neurol Sci       Date:  2021-05-29       Impact factor: 4.553

  6 in total

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